Canonical Allele Identifier: CA2773276766

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373446_139373463del , CM000668.2:g.139373446_139373463del	GRCh38
NC_000006.11:g.139694583_139694600del , CM000668.1:g.139694583_139694600del	GRCh37
NC_000006.10:g.139736276_139736293del	NCBI36
NG_016169.1:g.6186_6203del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.482_499del MANE Select	ENSP00000356623.2:p.Ser161_Pro167delinsThr
ENST00000367651.3:c.482_499del	ENSP00000356623.2:p.Ser161_Pro167delinsThr
ENST00000536159.2:c.482_499del	ENSP00000442831.1:p.Ser161_Pro167delinsThr
ENST00000537332.2:c.497_514del	ENSP00000444198.2:p.Ser166_Pro172delinsThr
ENST00000618718.1:c.476+6_476+23del	ENSP00000479918.1:n.476+6_476+23del
NM_001168388.2:c.482_499del	NP_001161860.1:p.Ser161_Pro167delinsThr
NM_001168389.2:c.497_514del	NP_001161861.2:p.Ser166_Pro172delinsThr
NM_006079.4:c.482_499del	NP_006070.2:p.Ser161_Pro167delinsThr
NM_006079.5:c.482_499del MANE Select	NP_006070.2:p.Ser161_Pro167delinsThr
NM_001168388.3:c.482_499del	NP_001161860.1:p.Ser161_Pro167delinsThr
NM_001168389.3:c.497_514del	NP_001161861.2:p.Ser166_Pro172delinsThr